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Research 481–510 of 812
- Microscopic Study concerning Hair Form of One Family in the Mixed Blood between European and Ponapean
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Healing hair naturally: A focus on herbal treatment for hair disorders
- Oral Presentations
- Do you know this syndrome? * Você conhece esta síndrome? *
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- 1017 The prostaglandin F2α analog bimatoprost activates secondary hair germ cells to promote hair growth through two distinct signaling pathways
- Liposomes enhance the hair follicle delivery of minoxidil sulfate with improved treatment of androgenic alopecia
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis
- Diffuse Hair Loss
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Expert consensus on the management of telogen effluvium in India
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Bitemporal hair loss related to traction alopecia
- Scarring Alopecia in Pediatric Patients: A Narrative Review of Etiologies, Diagnosis, and Management Strategies
- Prostaglandin F2α stimulates the growth of human intermediate hair follicles in ex vivo organ culture with potential clinical relevance
- Bimatoprost
- Diagnosis and Management of Hair Loss in Pediatric
- An analytical study of serum ferritin, vitamin D, and thyroid function in females with diffuse hair loss
- An Approach to Detect Alopecia Areata Hair Disease Using Deep Learning
- Androgenetic Alopecia (AGA)
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Telogen Effluvium: A Review
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.